Works matching IS 14337851 AND DT 2006 AND VI 45 AND IP 9
Results: 37
Nonlinear Effects in Rh-Catalyzed Asymmetric Olefin Hydrogenation Using Mixtures of Chiral Monodentate P LigandsWe thank the Fonds der Chemischen Industrie for generous support and Nils Theyssen for advice in measuring the hydrogenation rates.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1412, doi. 10.1002/anie.200503604
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Preview: Angew. Chem. Int. Ed. 9/2006.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1483, doi. 10.1002/anie.200690031
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Graphical Abstract: Angew. Chem. Int. Ed. 9/2006.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1334, doi. 10.1002/anie.200690030
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Bioorganic Chemistry: K. Sandhoff, H. Kessler, F. Diederich, and K. C. Nicolaou awarded.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1346, doi. 10.1002/anie.200600226
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Handbook of Reagents for Organic Synthesis. Reagents for High-Throughput Solid-Phase and Solution-Phase Organic Synthesis. Edited by Peter Wipf.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1347, doi. 10.1002/anie.200585319
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Remote Chiral Induction in the Organocatalytic Hydrosilylation of Aromatic Ketones and KetiminesWe thank the GSK and EPSRC for an industrial CASE awards to A.J.P.S.L., the Ministry of Education and Science of Spain for a postdoctoral fellowship to P.R.-L., the Socrates Exchange program, and Dr. Alfred Bader and the University of Glasgow for an additional support.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1432, doi. 10.1002/anie.200503941
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Cover Picture: Asymmetric Intramolecular Crossed-Benzoin Reactions by N-Heterocyclic Carbene Catalysis (Angew. Chem. Int. Ed. 9/2006).
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1327, doi. 10.1002/anie.200690029
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Asymmetric Intramolecular Crossed-Benzoin Reactions by N-Heterocyclic Carbene CatalysisThis work was supported by the Deutsche Forschungsgemeinschaft (Schwerpunktprogramm Organokatalyse) and the Fonds der Chemischen Industrie. We thank Degussa AG, BASF AG, Bayer AG, and Wacker Chemie for the donation of chemicals.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1463, doi. 10.1002/anie.200503885
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Chemistry—An Asian Journal: Lift-Off in Hawaii.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1330, doi. 10.1002/anie.200600208
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Circular-Polarization-Induced Enantiomeric Excess in Liquid Crystals of an Achiral, Bent-Shaped Mesogen.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1382, doi. 10.1002/anie.200503767
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How Does the Initial Alignment of Mesogens Affect the Photoinduced Bending Behavior of Liquid-Crystalline Elastomers?
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1378, doi. 10.1002/anie.200503684
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Electrochemical Enol Ether/Olefin Cross-Metathesis in a Lithium Perchlorate/Nitromethane Electrolyte SolutionThis work was partially supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science, and Technology and the Japan Society for the Promotion of Science.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1461, doi. 10.1002/anie.200503656
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Heterocyclic CarbenesThis work was supported by the Deutsche Forschungsgemeinschaft (SFB 424) and the International Graduate College “Template-Directed Chemical Synthesis” (GRK 673).
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1348, doi. 10.1002/anie.200503858
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In Situ Imaging of Electrochemically Induced Oxygen Spillover on Pt/YSZ CatalystsWe thank L. Gregoratti, A. Barinov, and M. Kiskinova (Sincrotrone ELETTRA, Trieste, Italy) for their invaluable support. We gratefully acknowledge the support of C. Korte for establishing the PLD technique and of L. Majdandzic in sample preparation. Financial support by the DFG (German Science Foundation) and the FCI (Fund of the German Chemical Industry) and the state of Hessia is also acknowledged.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1473, doi. 10.1002/anie.200503708
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Tetraarylphosphonium Salts as Solubility-Control Groups: Phosphonium-Supported Triphenylphosphine and Azodicarboxylate ReagentsThis work was supported by Valorisation-Recherche Québec (VRQ), Valorisation-Recherche s.e.c. (Univalor), and the Université de Montréal. A.A.B. is grateful to the NSERC (PGF B) and FCAR (B2) for postgraduate fellowships.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1415, doi. 10.1002/anie.200503599
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Amino Acid Derived Macrocycles—An Area Driven by Synthesis or Application?
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1364, doi. 10.1002/anie.200503428
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Dye-Sensitizer Effects on a Pt/KTa(Zr)O3 Catalyst for the Photocatalytic Splitting of WaterThe authors are grateful for financial support from the Nissan Science Research Foundation.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1420, doi. 10.1002/anie.200503316
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Inhibitors of HIV-1 Protease by Using In Situ Click ChemistryWe thank the National Institute of General Medical Sciences, the National Institutes of Health (GM048870), the Skaggs Institute for Chemical Biology, and the W. M. Keck Foundation (K.B.S.) for financial support.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1435, doi. 10.1002/anie.200502161
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Polyhedral Interconversion Coupled with Proton Transfer between an Ammonium Cation and the [Co(CO)4]− IonWork supported by the Dirección General de Investigación (MCyT), projects CTQ2005-08123-C02-01/BQU, and −02/BQU.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1457, doi. 10.1002/anie.200503597
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1,8-Bis(dimethylamino)naphthalene-2,7-diolate: A Simple Arylamine Nitrogen Base with Hydride-Ion-Comparable Proton AffinityThis work was in part supported by the Russian Foundation for Basic Research (grants RFBR No's 05-03-32110, 04-03-32538 and N. Sh. 945.2003.03). We thank Dr. A. G. Starikov, Rostov-on-Don, for computational assistance.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1453, doi. 10.1002/anie.200503472
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Synthesis of Functionalized Cyclopentenes through Catalytic Asymmetric [3+2] Cycloadditions of Allenes with EnonesWe thank Luke Firmansjah and Dr. Peter Mueller for assistance (X-ray crystallography) and the Jamison group for a sample of (R)-nmdpp. Support has been provided by the NIH (National Institute of General Medical Sciences: R01-GM57034; National Cancer Institute: training grant CA009112), Merck Research Laboratories, and Novartis. Funding for the MIT Department of Chemistry Instrumentation Facility has been furnished in part by NSF CHE-9808061 and NSF DBI-9729592.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1426, doi. 10.1002/anie.200503312
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Enhanced Collective Electron Transport by CdSe Quantum Dots Confined in the Poly(4-vinylpyridine) Nanodomains of a Poly(styrene-b-4-vinylpyridine) Diblock Copolymer Thin FilmThe authors acknowledge the National Science Council in Taiwan for funding (NSC 94-2120M-009-001).
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1449, doi. 10.1002/anie.200503152
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A Highly Regioselective Salt-Free Iron-Catalyzed Allylic AlkylationFinancial support by the Fonds der Chemischen Industrie, the Deutsche Forschungsgemeinschaft, the Otto-Röhm-Gedächtnisstiftung, and the Fonds zur Förderung des wissenschaftlichen Nachwuchses im Fachbereich Chemie der Universität Dortmund is gratefully acknowledged.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1469, doi. 10.1002/anie.200503274
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Laser-Induced Acoustic Desorption Mass Spectrometry of Single BioparticlesThis work was supported by grants from the Academia Sinica and the National Science Council (grant no. NSC 92-3112-B-001-012-Y) of Taiwan. We thank Y.-Y. Cheng for donating anemic blood samples, C. S. Chung for virus preparations, and Prof. Y. T. Lee for stimulating discussions.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1423, doi. 10.1002/anie.200503271
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Emission Enhancement by Formation of Aggregates in Hybrid Chromophoric Surfactant Amphiphile/Silica NanocompositesWe thank the National Science Council of the Republic of China (NSC94-2129M009-009) for financial support.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1404, doi. 10.1002/anie.200503067
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Label-Free Biosensing with Hydrogel MicrolensesL.A.L. acknowledges support from a Sloan Fellowship and a Camille Dreyfus Teacher–Scholar Award.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1446, doi. 10.1002/anie.200503102
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Pentarylene- and Hexarylenebis(dicarboximide)s: Near-Infrared-Absorbing Polyaromatic DyesWe gratefully acknowledge BASF AG and the Deutsche Forschungsgemeinschaft (Sonderforschungsbereich 625) for financial support, as well as Dr. R. Sens and Dr. C. Lennartz (BASF AG) for their calculations.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1401, doi. 10.1002/anie.200502998
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A Microporous Metal–Organic Framework for Gas-Chromatographic Separation of AlkanesThis work was supported by the University of Texas-Pan American through a Faculty Research Council award to B.C., by the Welch Foundation grant (BG-0017) to the Department of Chemistry at UTPA, by an appointment to the Higher Education Research Experiences (HERE) at the Oak Ridge National Laboratory (ORNL) for faculty (B.C.), which is sponsored by the US Department of Energy and administered by the Oak Ridge Institute for Science and Education, and by the Office of Basic Energy Sciences, US Department of Energy, under contract No. DE-AC05-00OR22725 with UT-Battelle, LLC (S.D.). We thank Dr. Jing-Feng Huang for his help with the GC separation of alkanes.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1390, doi. 10.1002/anie.200502844
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The Chlorination of the [Al13]− Cluster and the Stepwise Formation of Its Intermediate Products, [Al11]−, [Al9]−, and [Al7]−: A Model Reaction for the Oxidation of Metals?This work was financially supported by the Deutsche Forschungsgemeinschaft (Center for Functional Nanostructures, CFN), by the “Fonds der Chemischen Industrie”, and by the Air Force Office of Scientific Research (K.B.).
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1476, doi. 10.1002/anie.200502957
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Acid-Induced Conversions in Open-Framework Semiconductors: From [Cd4Sn3Se13]6− to [Cd15Sn12Se46]14−, a Remarkable Disassembly/Reassembly ProcessFinancial support from the National Science Foundation (DMR-0443785 and CHE-0211029 Chemistry Research Group) is gratefully acknowledged.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1397, doi. 10.1002/anie.200502787
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The Origin of the Halogen Effect on Reactivity and Reversibility of Diels–Alder Cycloadditions Involving FuranWe are grateful to the National Science Foundation and the Partnerships for Advanced Computational Infrastructure (PACI) for financial support of this research. The computations were performed on the National Science Foundation Terascale Computing System at the Pittsburgh Supercomputing Center (PSC) and on the UCLA Academic Technology Services (ATS) Hoffman Beowulf cluster. We are grateful to Albert Padwa and Michael E. Jung for discussions.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1442, doi. 10.1002/anie.200502677
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An Allosterically Regulated Molecular ShuttleThis work was supported by the European Union Future and Emerging Technology Program Hy3M and the EPSRC. D.S.M. is a Marie Curie Fellow; D.A.L. is an EPSRC Senior Research Fellow and holds a Royal Society–Wolfson Research Merit Award.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1385, doi. 10.1002/anie.200502624
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Regioselective Carbon–Carbon Bond Formation Reactions between TCNE or TCNQ and a Quinonoid RingThis work was supported by the Centre National de la Recherche Scientifique, the Ministère de la Recherche et des Nouvelles Technologies, and Clariant. We thank Prof. R. Welter and Dr. A. DeCian (ULP, Strasbourg) for the determination of the crystal structures, Dr. G. Royal (UJF, Grenoble) for preliminary electrochemical studies on compound 1 b, and the referees for constructive comments. TCNE=tetracyanoethylene, TCNQ=7,7′,8,8′-tetracyanoquinodimethane.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1393, doi. 10.1002/anie.200502574
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Thermal [2+2] Intramolecular Cycloadditions of Fuller-1,6-enynesThese investigations were financially supported by the MEC of Spain (Projects BQU2002-00855 and BQU2002-0412-C02-02). S.F. thanks the CAM for a postdoctoral contract. M.A. and M.G. thank the MEC for research grants.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1439
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Site-Selective Protein Immobilization by Staudinger LigationThis research was supported by the Volkswagen Stiftung, the Max Planck Gesellschaft, and the Fonds der Chemischen Industrie.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1408, doi. 10.1002/anie.200502057
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Photochemical Approach to Probing Different DNA Structures.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1354, doi. 10.1002/anie.200501962
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Enantioselective Synthesis of 2-Aryl Cyclopentanones by Asymmetric Epoxidation and Epoxide RearrangementWe are grateful for generous financial support from the General Medical Sciences of the National Institutes of Health (GM59705-06).
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- Angewandte Chemie International Edition, 2006, v. 45, n. 9, p. 1429, doi. 10.1002/anie.200501520
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